Device for analyzing a sample

ABSTRACT

This invention provides a device for analyzing a sample which is capable of performing rapid and precise analysis of a small amount of sample, and whose gradient in a measuring apparatus is not limited. This device comprises approximately a rectangular plate shaped body comprising a base member made of resin and a transparent covering. A first depressed cylindrical concave portion is formed in the upper surface of the base member, and a groove is formed in communication with the first depressed cylindrical concave portion, the groove extending to the end of the protrusion portion  5   c , and a second depressed cylindrical concave portion which is smaller than the first depressed cylindrical concave portion is formed in a certain position in the groove, the end of the groove opening to the outside at the end of the protrusion portion  5   c . Then, the transparent covering is placed over the upper surface of the base member and then integrated together. As a result, the first depressed cylindrical concave portion, the groove, the second depressed cylindrical concave portion, and the opening at the end of the groove are formed into a suction pressure generating chamber, a drawing channel, an analytical section, and an opening for drawing a sample, respectively.

This application is a Continuation of application Ser. No. 08/847,745,filed Apr. 22, 1997, now U.S. Pat. No. 6,001,307, which application(s)are incorporated herein by reference.

FIELD OF THE INVENTION

This invention relates to devices for analyzing samples such as bodyfluids, to methods for analyzing samples by using such devices, and toapparatuses for analyzing samples using such devices.

BACKGROUND OF THE INVENTION

There are various types of samples in the field of analytical chemistry,and particularly in the medical field, body fluids such as blood, urine,spinal fluid, saliva and the like, are important objects for analysis.There are needs for analyzing such samples in large amount andcollectively.

In order to meet such needs, a device for analyzing a sample having areagent film previously impregnated with a reagent, which is stuck on astrip, has been developed and practically used. In such a device, thereagent film is supplied with a sample such as blood, where a componentin the sample is reacted with the reagent to generate a pigment, wherebya color is developed in the reagent film, and the color is analyzed byusing an optical measuring apparatus such as a densitometer. By usingsuch a device, operations for preparing a reagent and reacting thereagent with a component in the sample can be simplified, thereby thewhole process for analyzing a sample becomes a routine exercise.

In such a device, examples of methods for supplying the reagent filmwith a sample include, methods utilizing capillarity, spotting, dipping,and the like. Among these methods, methods utilizing capillarity havebeen most commonly used. Because it is required to intercept externallight during optical measuring, it is necessary that a sample supplyingportion and an analytical section should be positioned away from eachother when the device is set in an optical measuring apparatus.Accordingly, a sample is required to be transferred in the device,therefore capillarity is utilized as a means for transferring thesample. Examples of devices utilizing capillarity are those disclosed inJapanese Patent Application Laid-open No. Hei 4-188065 or in JapanesePatent Application Laid-open No. Sho 57-132900.

FIG. 22 shows a device for analyzing a sample utilizing capillarity. Asshown in the drawing, the device comprises a triangular shaped samplingpoint 42 protruding from an approximately center portion of the frontface 44 of a transparent base member 47 made of acrylic resin, a groove46 extending from the sampling point 42 toward the back portion of thebase member 47, and a slot 45 formed as an extension of the groove.Furthermore, a reagent film 48 is stuck on the upper face of the basemember 47 on the side of the front face 44, so that it may cover overthe groove 46. The structure of the reagent film 48 is determined asappropriate depending upon the type of a sample. For example, whenanalyzing plasma components of blood, a reagent film having a laminatedstructure comprising a filtration layer, a reagent layer, a transparentprotective layer, and an opaque protective layer, which are laminated inthis order from the bottom, in which an observation window 50 is formedfor entering light in an approximately center portion of the opaqueprotective layer, is used.

A sample may be analyzed by using such a device as in the followingsteps. First, a drop of blood is obtained from a subject and broughtinto contact with the sampling point 42. Then, the blood is introducedinto the groove 46 by capillarity and the whole groove is filled withthe blood. When the blood permeates into the reagent film 48 coveringover the upper portion of the groove 46, erythrocytes are first removedby the filtration layer, and plasma components reach the reagent layer,where a pigment is generated through a reaction between a reagent in thereagent layer and a component in the plasma, whereby a color isdeveloped in the reagent layer. In this state, the device is set in anoptical measuring apparatus such as a densitometer, where the colordeveloped in the reagent layer may be measured by irradiating light fromthe observation window 50.

However, there are problems as described below in using a deviceutilizing capillarity.

First, because a capillary channel is required to be continuously filledwith a sample in order to cause capillarity, an amount of a sample morethan required for analysis is needed. In addition, it takes some time tointroduce a sample by capillarity, so that measuring cannot be performedquickly. Furthermore, in body fluids such as blood, there aredifferences among individuals in properties such as viscosity, whichaffect capillarity, therefore the time period required for introducing asample into the analytical part or the like cannot be fixed. As aresult, it is difficult to fix a time period required for analysis, suchas time for reaction with a reagent. Accordingly, there is a possibilitythat an error might be caused in analysis results. Furthermore, sincethe drawing force by capillarity is very weak, it is easily affected bygravitational force. Therefore, when introducing a sample, the gradientof the device should be restricted, and the structure of an opticalmeasuring apparatus should also be limited. Furthermore, the samplesupplying portion and the analytical section cannot be positioned apartfrom each other because of the weakness of the drawing force ofcapillarity, so that possibilities of contamination during anintroduction of a sample or influence of external light cannot becompletely eliminated in an optical measuring apparatus.

On the other hand, the spotting method has a disadvantage in that whenusing blood as the sample, the sampling spot is limited to a fingertip,and sampling from an ear or the abdomen is difficult.

SUMMARY OF THE INVENTION

The present invention has been developed in view of the above mentionedbackground, and an object of the invention is to provide a devicecapable of performing a rapid and precise analysis of a small amount ofa sample, a method for analyzing a sample using such a device, and anapparatus for analyzing a sample using such a device.

In order to solve the above-mentioned problems, the present inventionprovides a device for analyzing a sample comprising a suction pressuregenerating means, a drawing channel in communication with the suctionpressure generating means, an analytical section formed in a certainposition in the drawing channel, and an opening formed at the end of thedrawing channel, wherein a sample is introduced from the opening andthen drawn into the analytical section through the drawing channel bythe suction pressure developed by the suction pressure generating means.

Accordingly, in the device of the present invention, a sample is drawnforcefully by utilizing suction pressure in place of capillarity as usedin a conventional device. That is, a suction pressure is developed bythe suction pressure generating means, a sample is introduced into theopening by the suction pressure, then the sample is drawn by the suctionpressure through the drawing channels into the analytical section, wherethe sample is analyzed by an optical means, an electrochemical means, orthe like. Thus, by using a suction pressure to draw a sample forcefully,it is ensured that a small amount of a sample is introduced into theanalytical section. In addition, the time period required forintroducing the sample can be fixed to a certain short time,irrespective of the properties of the sample such as viscosity.Accordingly, for example, when analyzing a sample by using a reagent,the time period for reaction between a component in a sample and areagent can be fixed. In addition, by drawing a sample forcefully, forexample, the amount of a sample which is reacted with a reagent can beconstantly fixed. Accordingly, errors which might be caused in analysisresults can be prevented.

Furthermore, since a sample is drawn forcefully in the device of thepresent invention, it is not necessary to limit the distance between thesample supplying portion and the analytical section. Therefore, in thedevice of the present invention, the distance between the samplesupplying portion and the analytical section can be longer than in adevice utilizing capillarity. Accordingly, influence of external lightcan be eliminated in an optical measuring apparatus. Therefore, by usingthe device of the present invention, a small amount of a sample can beanalyzed rapidly and precisely. Furthermore, because the sample is drawnforcefully, the influence of gravitational force can be nearly ignored.

In the present invention, by “suction pressure” is understood a pressurefor drawing a sample, which is usually a negative pressure.

A sample used in the present invention is not particularly limited aslong as it can be sucked, and liquids, sols, or the like are included inthe examples. Furthermore, examples of a sample which may be analyzed inthe present invention include, whole blood, urine, spinal fluid, bloodplasma, serum, saliva, or the like.

Method for analyzing a sample using the device of the present inventionare not particularly restricted. For example, an optical means, anelectrochemical means or the like can be applied in such methods.

When optical measuring means is applied, either a reagent which reactswith a component in a sample to generate a pigment, or a reagent whichreacts with a component in a sample to represent a color in itself isgenerally used. However, there are some cases in which an analysis maybe conducted by using only light transmissivity or light reflectance andwithout using a reagent. One example of such a case is when analyzing ahematocrit value of blood. Furthermore, instead of measuring transmittedlight, other optical means such as measuring reflected light,fluorescence or the like may also be applied.

When electrochemical means is applied, a change in electric current orin electric potential caused by the oxidation-reduction reaction of thesample may be usually measured, and a reagent which causes anoxidation-reduction reaction when reacted with a component in a sampleis normally used in such a measurement.

The reagent used in the present invention may be either a dry-type orwet-type reagent. Furthermore, in a device for simultaneous analysis ofmultiple items (hereinafter referred to as “multiple analysis”) asdescribed later, various types of reagents may be usually used dependingupon the number of items to be analyzed.

It is preferable that the device of the present invention comprises aplurality of drawing channels, in each of which an analytical section isformed in a certain position, the ends of the drawing channels mergingand forming one opening. By using a device having such a structure,simultaneous analysis of multiple items, namely multiple analysis, canbe achieved. Such a device is referred to as a device for multipleanalysis.

Although suction pressure is utilized for drawing a sample forcefully inthe present invention, a suction pressure may also be used incombination with capillarity as described later.

A device for analyzing a sample provided with a bypass channel, and adevice for analyzing a sample in which a stopper which is gas-permeableand liquid-impermeable is formed, are preferred embodiments of thepresent invention. As described above, the device of the presentinvention has many advantages by utilizing suction pressure for drawinga sample forcefully. However, because such a forced sucking is markedlystrong compared to a sucking utilizing capillarity, there is apossibility that a sample might pass through the analytical section anddoes not remain there. The above embodiments of the present inventionprovide a solution for such a problem. When using either of theabove-described embodiments of the present invention, it is notnecessary to be particularly careful when generating a suction pressure,therefore allowing simpler manipulation.

Accordingly, in a first preferred embodiment, a device for analyzing asample of the present invention includes a suction pressure generatingmeans, a drawing channel in communication with the suction pressuregenerating means, an analytical section formed in a certain position inthe drawing channel, the end of the drawing channel forming an opening,and in addition provided with a bypass channel which branches from aportion of the drawing channel between the analytical section and theopening and is in communication with the suction pressure generatingmeans, wherein the relationship of the liquid flow resistance (X) in thedrawing channel between the analytical section and the suction pressuregenerating means, the liquid flow resistance (Y) in the bypass channel,and the liquid flow resistance (Z) in the drawing channel between thebranching portion of the bypass channel and the analytical section issuch that X>Y>Z.

In this embodiment, when the developed suction pressure is large, anexcess of suction pressure may still remain even after a sufficientamount of a sample has been introduced into the analytical section orthe like. In case that an excess of suction pressure remains, there arepossibilities that a sample which has been introduced into theanalytical section or the like might further be drawn into the suctionpressure generating means, that air might be entrained in the analyticalsection, or that a pigment generated through reaction between acomponent in the sample and a reagent might flow into the suctionpressure generating means. This first preferred embodiment solves suchproblems by providing a bypass channel, and also by having therelationship of the liquid flow resistance (Y) in the bypass channel andthe liquid flow resistances (X, Z) in the two portions of the drawingchannel is such that X>Y>Z.

Accordingly, because the liquid flow resistance (Z) in the drawingchannel between the branching portion of the bypass channel and theanalytical section is the smallest among the three liquid flowresistances (X), (Y), and (Z), even if a suction pressure larger thanrequired is generated by the suction pressure generating means, a sampleis first introduced from the opening and drawn into the analyticalsection in a sufficient amount. In this case, even if an excess amountof a sample and/or entrained air are drawn by the excess suctionpressure, the excess of a sample and/or the entrained air can beintroduced into the bypass channel, while the sample introduced into theanalytical section, a generated pigment and the like remain in theanalytical section. This is because the liquid flow resistance (X) inthe drawing channel between the analytical section and the suctionpressure generating means is larger than the liquid flow resistance (Y)in the bypass channel. Then, the excess of a sample and the entrainedair may be discharged into the bypass channel or through the bypasschannel into the suction pressure generating means. Accordingly, even ifa large suction pressure is generated, it is ensured that a sample isintroduced into the analytical section to be analyzed, therefore furtherrapid and precise analysis of the sample can be achieved.

In the present invention, by “liquid flow resistance” is understood aresistance to flow to which liquid is subjected when moving through achannel, and serves as a criterion for ease of liquid flow.

Suitable methods for controlling the liquid flow resistance in each ofthe channels are, for example, changing the diameter of the channel,treating the inner surface of the channel which contacts with liquid byusing a detergent, a water repellent agent or the like in order tochange the wettability. Examples of the water repellent agents aresilicon, tetrafluoroethylene resin, and the like.

In order to perform multiple analysis as described above, it ispreferable that the first preferred embodiment of the present inventionis provided with a plurality of drawing channels, an analytical sectionformed in a certain position in each of the drawing channels, the endsof the respective drawing channels merging and forming one opening, anda bypass channel branching from a portion of the drawing channel betweenthe merging portion and the opening and being communicated with thesuction pressure generating means.

A second preferred embodiment comprises a suction pressure generatingmeans, a drawing channel in communication with the suction pressuregenerating means, an analytical section formed in a certain positionin-the drawing channel, an opening being formed at the end of thedrawing channel, and further comprising a stopper which is gas-permeableand liquid-impermeable (hereinafter referred to as a “stopper”) formedin a certain position in the drawing channel between the suctionpressure generating means and the analytical section, by which a flow ofa sample into the suction pressure generating means can be prevented.

In the second embodiments, the portion of the drawing channel betweenthe analytical section and the suction pressure generating means wherethe stopper may be formed should include both the boundary portionbetween the drawing channel and the suction pressure generating means,and the boundary portion between the drawing channel and the analyticalsection.

In the second embodiment, the stopper is usually made of a hydrophobicporous material.

It is preferable that the second embodiment be made for multipleanalysis as described below.

That is, in the second embodiment, it is preferable that a plurality ofanalytical sections are formed in certain position in the drawingchannel, and that a stopper is formed in a portion of the drawingchannel between the suction pressure generating means and the analyticalsection which is the closest to the suction pressure generating means.

Furthermore, it is preferable that the second embodiment be providedwith a plurality of drawing channels, and an analytical section formedin a certain position in each of the drawing. channels, the ends of therespective drawing channels merging and forming one opening.

It is preferable that the opening of the drawing channel is enlargedtoward the end, that is, funnel-shaped. By having such a shape, a samplesuch as blood can be retained in the opening after the sample isintroduced, therefore subsequent drawing operation becomes easier. Inaddition, air inclusion can also be reduced. Especially in case ofsampling blood from a small spot such as a fingertip, it is required toensure that the opening for the drawing channel in the device iscontacted with the sampling spot until introduction of the sample iscompleted. Therefore, substantial attention is required for controllingsampling, resulting in more complex operation. Furthermore, since anamount of blood which can be obtained from a fingertip or the like is aslittle as several 10 μl air inclusion may easily occur in a conventionaldevice for analyzing a sample during introduction of a sample, therebygreatly affecting the measured results. In order to solve such problems,the opening for the drawing channel is formed into a funnel-shape, sothat the sample can be retained there. By having such a structure, it ispossible to draw the sample through the channel after detaching theopening from the sampling spot, therefore a sample can be easilyobtained from a small spot without causing air inclusion.

Furthermore, it is also preferable that the device be provided with aliquid pooling portion formed between the opening and the drawingchannel, and an air vent passage branching from a portion of the drawingchannel between the liquid pooling portion and the analytical section,the end of the air vent passage opening to the outside of the device.The air vent passage branches from a portion of the drawing channelbetween the liquid pooling portion and the analytical section so thatair inclusion can be prevented during introduction of the sample.

By providing such a liquid pooling portion and an air vent passage, asample can be introduced by capillarity developed by the air ventpassage and retained in the liquid pooling portion, therefore subsequentsucking operation can be performed without causing air inclusion afterdetaching the opening from the sampling spot.

It is preferable that the liquid flow resistance in the air vent passageis larger than that in the liquid pooling portion, so that air inclusioncan be further prevented.

Suitable methods for controlling the liquid flow resistance are, forexample, changing the dimension of a cross section, treating the surfacewhich contacts with liquid by using a surface active agent, a waterrepellent agent or the like to change the wettability. Examples of thewater repellent agent include silicon, tetrafluoroethylene resin, andthe like. It is preferable that the liquid flow resistance should becontrolled by changing dimensions of a cross section in view ofcontrollability. For example, the thickness and the width of the liquidpooling portion may be formed larger than those of the air vent passage.

In the device of the present invention, the analytical section formed inthe drawing channel may serve both as a reagent positioning section anda reagent reaction section. Alternatively, a reagent positioningsection, a reagent reaction section, and an analytical section may beprovided independently in certain positions in the drawing channel.Still alternatively, a plurality of reagent reaction sections, reagentpositioning sections, and analytical sections may be provided in certainpositions in the drawing channel.

In the device of the present invention, an analytical section preferablyserves both as a reagent positioning section and as a reagent reactionsection. However, if a reagent can move through the drawing channel, areagent positioning section, a reagent reaction section, and ananalytical section (hereinafter also referred to as a “measuringsection”) may be independently formed in certain positions in thedrawing channel.

In such a device, a sample and a reagent can be mixed and stirred whilethe sample moves between each of the respective sections, and also incase of using a dry-type reagent, dissolution of the reagent may befacilitated. The reagent may move either independently or together withthe sample.

Furthermore, such a device can be applied for multiple steps reactionincluding a pre-treatment step. For example, if a plurality of reagentreaction sections or the like are provided in series in the drawingchannel, a sample can be transferred to the respective sections, whilecausing reactions respectively. By using such a device, for example, incase of performing analysis utilizing antigen-antibody reaction, inwhich B/F separation is required, B/F separation can be performed bytransferring a sample and a rinsing solution among the respectivereagent reaction sections or the like.

Furthermore, in case of using a reagent consisting of two or morecomponents, which cannot be mixed prior to reaction with a sample, it ispreferred that a plurality of reagent positioning sections are providedin certain positions in the drawing channel.

Next, in the device for analyzing a sample of the present invention, asuction pressure generating chamber, a suction pressure generating tubeor the like capable of changing the volume, may be used as a suctionpressure generating means. A vent may be formed in the suction pressuregenerating chamber.

With regard to the suction pressure generating tube, a suction pressureis generated by drawing the tube through a hand.

In the device of the present invention, when analyzing a sample by usingan electrochemical means, it is preferable that the analytical sectionis provided with a pair of electrodes comprising a working electrode anda counter electrode.

According to another aspect of the present invention, a method foranalyzing a sample comprises preparing the device of the presentinvention, generating a suction pressure by the suction pressuregenerating means, thereby introducing a sample into the opening, anddrawing the sample by the suction pressure through the drawing channelinto the analytical section, where analysis of the sample is performed.

A method for analyzing a sample using the first or the second embodimentof the present invention will be described.

A method for analyzing a sample using the first embodiment of the deviceof the present invention comprises the steps of preparing the firstembodiment, developing a suction pressure by the suction pressuregenerating means, thereby introducing a sample into the opening, anddrawing the sample by the suction pressure through the drawing channelinto the analytical section, while excess amount of the sample and/orentrained air are discharged into the bypass channel and also throughthe bypass channel into the suction pressure generating means, thereuponperforming an analysis of the sample.

A method for analyzing a sample using the second embodiment comprisesthe steps of preparing the second embodiment, developing a suctionpressure by the suction pressure generating means, thereby introducing asample into the opening, drawing the sample by the suction pressurethrough the drawing channel into the analytical section, where analysisof the sample is performed.

When multiple analysis is conducted in these methods, multiple items maybe simultaneously analyzed by using a device for multiple analysis.

These methods for analyzing a sample, in which either a device having afunnel-shaped opening or a device provided with a liquid pooling portionand an air vent passage is used, comprise the steps of preparing thedevice for analyzing a sample, contacting the opening with a sample,thereby drawing the sample into the opening or into the liquid poolingportion by capillarity to retain the sample, and then generating asuction pressure by the suction pressure generating means, drawing thesample retained in the opening or in the liquid pooling portion by thesuction pressure through the drawing channel into the analyticalsection, where analysis of the sample is performed.

According to the method for analyzing a sample using either a deviceprovided with a funnel-shaped opening or a device in which a liquidpooling portion and an air vent passage are formed, for example, thedevice can be detached from a sampling spot after contacting the openingwith a sample in the sampling spot to introduce the sample into theopening or into the liquid pooling portion, where the sample isretained, therefore making the subsequent sucking operation easier.

In these methods for analyzing a sample of the present invention, themeans of analysis is not particularly limited, and for example, anoptical means or an electrochemical means is used.

Furthermore, apparatus for analyzing a sample of the present inventionmay be either an optical measuring apparatus or an electric measuringapparatus.

The optical measuring apparatus comprises an optical measuring systemprovided with a light irradiating section and a light detecting section,and a device for a analyzing a sample, wherein the device is positionedso that the analytical section of the device can be irradiated withlight from the light irradiating section, and so that the detectingsection can detect transmitted light, fluorescence, or reflected lightin the analytical section.

The electric measuring apparatus comprises an electric signal generatingmeans, an electric signal detecting means, and a device for analyzing asample, wherein the working electrode of the device and the electricsignal generating means are connected to each other, and the counterelectrode of the device and the electric signal detecting means areconnected to each other.

BRIEF DESCRIPTION OF THE DRAWINGS

The above and other objects, features and advantages of the presentinvention will be apparent from the following detailed description ofthe preferred embodiments of the invention in conjunction with theaccompanying drawings, in which:

FIG. 1(A) is a plan view of one embodiment of the device for analyzing asample of the present invention, and FIG. 1(B) is a cross-sectional viewof the device of the FIG. 1(A) taken along the line I—I.

FIG. 2 is a plan view of another embodiment of the device of the presentinvention.

FIG. 3 is a plan view of still another embodiment of the device of thepresent invention.

FIG. 4 is a plan view of still another embodiment of the device of thepresent invention.

FIGS. 5(A)-5(D) are plan views showing a stepwise process for drawing asample in one embodiment of the device of the present invention in whicha bypass channel is provided.

FIG. 6(A) is a plan view of still another embodiment of the device ofthe present invention, and FIG. 6(B) is a cross-sectional view of thedevice of the FIG. 6(A) taken along the line II—II.

FIG. 7 is a plan view of still another embodiment of the device of thepresent invention.

FIG. 8 is a plan view of still another embodiment of the device of thepresent invention.

FIG. 9(A) is a plan view of still another embodiment of the device ofthe present invention, and FIG. 9(B) is a cross-sectional view of thedevice of the FIG. 9(A) taken along the line III—III.

FIG. 10 is a perspective view showing the fabrication of the deviceshown in FIG. 9.

FIG. 11(A) is a plan view of the device shown in FIG. 9, in which asample is introduced and retained in the liquid pooling portion, andFIG. 11(B) is a plan view of the device shown in FIG. 9, in which asample is drawn into the analytical section.

FIG. 12 is a plan view of still another embodiment of the device of thepresent invention.

FIG. 13 is a plan view of still another embodiment of the device of thepresent invention.

FIG. 14 is a plan view of still another embodiment of the device of thepresent invention.

FIG. 15 is a plan view of still another embodiment of the device of thepresent invention.

FIG. 16 is a plan view of still another embodiment of the device of thepresent invention.

FIG. 17(A)-(D) are cross-sectional views showing a process for drawing asample in a still another embodiment of the device of the presentinvention.

FIG. 18(A)-(D) are cross-sectional views showing a process for drawing asample in a still another embodiment of the device of the presentinvention.

FIG. 19(A) is a plan view showing a still another embodiment of thedevice of the present invention, and Figure 19(B) is a cross-sectionalview of the device of the FIG. 19(A) taken along the line IV—IV.

FIG. 20 is a perspective view showing the fabrication of the deviceshown in FIG. 19.

FIG. 21(A)-(H) are plan views showing an analysis using a still anotherembodiment of the device of the present invention.

FIG. 22 is a perspective view of a conventional device for analyzing asample.

DESCRIPTION OF EMBODIMENTS OF THE INVENTION

Next, embodiments of the present invention will be described. In thefollowing embodiments, unless particularly shown otherwise, theanalytical section serves both as a reagent positioning section and areagent reaction section.

EXAMPLE 1

FIG. 1 shows an embodiment of a device for analyzing a sample of thepresent invention. FIG. 1(A) is a plan view showing such a device, andFIG. 1(B) is a cross-sectional view showing the device of FIG. 1(A)taken along the line I—I.

As shown in the drawings, one end portion of the rectangular plateshaped body 5 (i.e. the left end portion in the drawings) is formed intoa protrusion portion 5 c which has a smaller width than that of thebody. The width of the protrusion portion 5 c is decreasing toward theend. Furthermore, the body 5 comprises a base member 5 b and a covering5 a which covers over the base member. The base member 5 b and thecovering 5 a are usually integrated together by using an adhesive suchas a hot melt adhesive.

In the upper surface side of the base member 5 b, a first depressedcylindrical concave portion, which forms a suction pressure generatingchamber, is formed in a portion on one end side (right side in thedrawings) relative to the center portion, a groove which forms a drawingchannel 2 is formed in communication with the first depressedcylindrical concave portion, the groove extending to the end of theprotrusion portion 5 c, a second depressed cylindrical concave portionwhich is smaller than the first depressed cylindrical concave portion,which will form an analytical section 3, is formed in a certain positionin the groove at an approximately center portion of the body 5, andfurther the end of the groove opens to the outside at the end of theprotrusion portion 5 c, thereby forming an opening 4 for drawing asample. Then, by covering the surface of the base member 5 b with acovering 5 a and integrating both of them together, the first depressedcylindrical concave portion, the groove, the second depressedcylindrical concave portion, and the end of the groove become thesuction pressure generating chamber 1, the drawing channel 2, theanalytical section 3, and the opening 4, respectively.

Furthermore, in subsequent embodiments, a suction pressure generatingchamber, a drawing channel, a bypass channel, and the like are formed byforming depressed cylindrical concave portions and a groove as in thisembodiment.

Although a reagent is not shown in the drawings, when the covering 5 ais transparent and light may be irradiated through the covering (fromthe side of the covering), for example, a reagent film impregnated witha reagent may be stuck on the inner surface of the covering 5 acorresponding to the analytical section 3. Furthermore, in the drawings,2 a refers to the portion of the drawing channel 2 between the opening 4and the analytical section 3, and 2 b refers to the portion of thedrawing channel 2 between the analytical section 3 and the suctionpressure generating chamber 1, respectively.

The dimensions of the device are usually 20 to 50 mm in overall length,10 to 30 mm in width, 1 to 5 mm in overall thickness, 10 to 20 mm inlength of the protrusion portion, 5 to 10 mm in maximum width of theprotrusion portion, and 3 to 5 mm in minimum width of the protrusionportion. Furthermore, the dimensions of the suction pressure generatingchamber 1 are usually 10 to 20 mm in diameter, 0.2 to 1 mm in depth, andthe dimensions of the analytical section 3 are usually 2 to 5 mm indiameter and 0.1 to 0.5 mm in depth. Furthermore, the dimensions of thedrawing channel 2 are usually 15 to 40 mm in overall length, 1 to 3 mmin width, and 0.1 to 0.5 mm in depth, in which the drawing channel 2 bbetween the suction pressure generating chamber 1 and the analyticalsection 3 is 5 to 20 mm in length, and the drawing channel 2 a betweenthe analytical section 3 and the opening 4 is 10 to 30 mm in length.

Examples of the material for the base member 5 b include acrylonitrilebutadiene styrene copolymer (ABS resin), polystyrene, Noryl resin,polyethylene, polyethylene terephthalate (PET), and acrylic resin. It isparticularly preferred to use polystyrene or acrylic resin in view oflight transmissivity and the like.

It is required that the covering 5 a have an elastic property. Moreover,when light is irradiated through the covering, it is also required thatat least the portion of the covering corresponding to the analyticalsection 3 should be transparent. Examples of suitable materials for thecovering are PET, polyethylene, and vinyl chloride. In particular, it ispreferred to use PET in view of processability and dimensions.

The reagent is usually contained in a reagent film as previouslydescribed, and the structure of the reagent film is determined asappropriate depending upon the type of the object for analysis. Forexample, when plasma components of blood is the object for analysis, areagent film having a structure in which a filtration layer forseparating erythrocytes, a reagent layer impregnated with a reagent, anda base member are laminated in this order is usually used. Furthermore,the reagent film is arranged in the analytical section 3 in such amanner that the filtration layer may contact with blood (the sample),and that irradiating light may enter from the side of the transparentprotective layer. In addition, conventionally known materials may beused for the respective layers of the reagent film.

For example, an analysis using this device may be conducted as follows.

First, the portion of the covering 5 a corresponding to the suctionpressure generating chamber 1 of the device is compressed by applying apressure, for example, by pressing with a finger.

Then, in this state, the opening 4 at the end of the protrusion portion5 c is contacted with a sample. Then, the pressure applied to thechamber is released by weakening the pressing force with a finger sothat the compressed portion of the covering 5 a can return to itsoriginal shape due to the elasticity of the covering. At this time, asuction pressure is generated, whereby the sample is introduced into theopening 4, and then the sample is further drawn through the drawingchannel 2 a into the analytical section 3. The time period required forintroduction of the sample into the analytical section 3 in this deviceis markedly short compared to a case of using a device utilizingcapillarity. In addition, such time is hardly affected by the propertiesof the sample such as viscosity. Then, a reaction between a component inthe sample and the reagent contained in the reagent film takes place inthe analytical section 3 to generate a pigment, whereby a color isdeveloped in the reagent film. Then, the device in which a color isdeveloped in the reagent film is set in a predetermined position in anoptical measuring apparatus such as a densitometer. Then, light isirradiated into the device through the covering 5 a, whereby when usingthe densitometer, a reflected light is detected in a detecting sectionto measure the developed color. When both the base member 5 b and thereagent film are also transparent, the sample can also be analyzed byusing transmitted light.

EXAMPLE 2

Next, FIG. 2 is a plan view showing an embodiment of a device formultiple analysis of the present invention. The device for multipleanalysis is capable of analyzing three items simultaneously.

As shown in the drawing, one end portion of the rectangular plate shapedbody 5 (the left end in the drawing) is formed into a protrusion portion5 c, which is smaller than the body in width in this device. The widthof the protrusion portion 5 c is decreasing toward the end. Furthermore,the body 5 comprises a base member and a covering which covers over thebase member in this device like in the predescribed embodiment.

Like in the device in Example 1, in the upper surface of the basemember, three drawing channels 2 b extend from a suction pressuregenerating chamber 1 formed in one end side portion of the body (rightside in the drawings) relative to the center of the body. At the end ofeach drawing channel 2 is formed an analytical section 3, differenttypes of reagents (not shown) being disposed in the respectiveanalytical sections 3, and three drawing channels 2 a extend from therespective analytical sections 3, the ends of the drawing channels 2 amerging and forming one opening 4. When the covering is transparent, thereagents are disposed by sticking reagent films on the portions of theinner surface of the covering corresponding to the respective analyticalsections 3.

In such a device for multiple analysis, overall dimensions aredetermined as appropriate depending upon the number of the items to beanalyzed. Because three items are analyzed in this embodiment, thedimensions of the device are usually 30 to 80 mm in overall length, 20to 50 mm in width, 1 to 5 mm in overall thickness, 10 to 20 mm in lengthof the protrusion portion, 5 to 10 mm in maximum width of the protrusionportion, 3 to 5 mm in minimum width of the protrusion portion.

Other things such as the materials, dimensions of the suction pressuregenerating chamber, the drawing channels and the like, are the same asin the predescribed embodiment of a device for analyzing a sample.Furthermore, the number of items to be analyzed is not particularlylimited; however, it is usually between 1 and 20, preferably between 3and 5. In such a case, various numbers of analytical sections anddrawing channels may be formed depending upon the number of the items tobe analyzed.

For example, an analysis using such a device for multiple analysis maybe performed as follows.

First, a portion of the covering 5 a corresponding to the suctionpressure generating chamber 1 of the device is compressed by applying apressure, for example, by pressing with a finger.

Then, in this state, the opening 4 at the end of the protrusion portionis contacted with a sample. Then, the applied pressure to the chamber isreleased by weakening the pressing force with a finger so that thecompressed portion of the covering may return to its original shape dueto the elasticity of the covering. At this time, a suction pressure isgenerated, whereby the sample is drawn into the opening 4 and thenfurther drawn through the three drawing channels 2 a to the threeanalytical sections 3. Like in the embodiment in Example 1, the timeperiod required for the introduction of the sample into the respectiveanalytical sections 3 in this device is markedly short compared to thatin a device using capillarity. In addition, the time is hardly affectedby the properties of the sample such as viscosity. Then, reactionsbetween components in the sample and the reagents contained in therespective reagent films take place to generate pigments in therespective analytical sections 3, whereby colors are developed in therespective reagent films. Then, the device in which colors are developedin the respective reagent films is set in a predetermined position in anoptical measuring apparatus such as a densitometer. Then, light isirradiated into the device, so that when using the densitometer, areflected light may be detected in a detecting section to measure thedeveloped color, so that three items can be analyzed simultaneously.

EXAMPLE 3

FIG. 3 shows a plan view of an embodiment of a device for analyzing asample of the present invention provided with a bypass channel.

As shown in the drawing, one end side portion of the rectangular plateshaped body 5 (the left end in the drawing) is formed into a protrusionportion 5 c, which is smaller than the body in width. The width of theprotrusion portion 5 c is decreasing toward the end. Furthermore, thebody 5 comprises a base member and a covering which covers over the basemember in the device like in the predescribed embodiment.

Like in the embodiment in Example 1, in the upper surface of the basemember 5 b, a drawing channel 2 b extends from a suction pressuregenerating chamber 1 formed in one end side portion of the body 5 (rightside in the drawing) relative to the center of the body. At the-end ofthe drawing channel 2 b is formed an analytical section 3, and a reagent(not shown) is disposed in the analytical section 3, and further adrawing channel 2 a extends from the analytical section 3 toward the endof the protrusion portion 5 c. At the end of the drawing channel 2 a isformed an opening 4. Where the covering is transparent, the reagent isdisposed by sticking a reagent film on a portion of the inner surface ofthe covering corresponding to the analytical section 3. A bypass channel6 branches from a portion of the drawing channel 2 a between the opening4 and the analytical section 3, and extends to communicate with thesuction pressure generating chamber 1.

Furthermore, the relationship among three liquid flow resistances,namely, the liquid flow resistance (X) in the drawing channel 2 bbetween the suction pressure generating chamber 1 and the analyticalsection 3, the liquid flow resistance (Y) in the bypass channel, and theliquid flow resistance (Z) in the drawing channel 2 a between thebranching portion of the bypass channel 6 and the analytical section 3is such that X>Y>Z.

As shown in the drawing, the entire drawing channel 2 a has a largediameter, so that the liquid flow resistance (Z) is the smallest amongthe three, the bypass channel 6 includes a certain length of a channel 6a having a small diameter extending from the branching portion, so thatthe liquid flow resistance (Y) is the second smallest, and the entiredrawing channel 2 b has a small diameter, so that the liquid flowresistance (X) is the largest.

The drawing channel 2 a is usually 10 to 30 mm in length, 1 to 3 mm inwidth, 0.1 to 0.5 mm in depth. The bypass channel 6 is usually 10 to 30mm in overall length, wherein the bypass channel 6 a having a smalldiameter is 0.5 to 5 mm in length, 0.1 to 0.5 mm in width, and 0.1 to0.5 mm in depth, and also the portion of the bypass channel having alarge diameter is 1 to 3 mm in width and 0.1 to 0.5 mm in depth. Thedrawing channel 2 b is usually 0.5 to 30 mm in length, 0.1 to 0.5 mm inwidth, and 0.1 to 0.5 mm in depth.

In such a device having the bypass channel 6, the overall dimensions,materials, dimensions of the suction pressure generating chamber and thelike, and so forth, are the same as those of the device in Example 1.

Next, FIG. 4 shows a plan view of an embodiment of a device having thebypass channel 6 in which the channel 6 a having a small diameter isrelatively long. In such a device, the bypass channel 6 is usually 10 to30 mm in overall length, wherein the bypass channel 6 a having a smalldiameter is 3 to 10 mm in length, 0.1 to 0.5 mm in width, and 0.1 to 0.5mm in depth, and also the portion of the bypass channel having a largediameter is 1 to 3 mm in width and 0.1 to 0.5 mm in depth. By havingsuch a relatively long bypass channel 6 a having a small diameter, it ispossible to provide a large difference between the liquid flowresistance (Y) in the bypass channel 6 and the liquid flow resistance(Z) in the drawing channel 2 a between the branching portion of thebypass channel 6 and the analytical section 3.

In the device shown in FIG. 4, the width of the opening 4 is increasingtoward the end, that is, funnel-shaped. By having such a shape, a samplecan be retained in the funnel-shaped opening 4 during sampling,therefore the subsequent sucking operation can be performed smoothly,while air inclusion can be prevented. The opening 4 is usually 3 to 6 mmin maximum width, 1 to 3 mm in minimum width, and 1 to 5 mm in length.

Other than the bypass channel 6 and the opening 4, the structure of thedevice shown in FIG. 4 is the same as that of the device shown in FIG.3.

An analysis using such a device having a bypass channel (FIG. 3 or 4) isconducted, for example, as follows.

First, a portion of the covering corresponding to the suction pressuregenerating chamber 1 of the device is compressed by applying a pressure,for example, by pressing with a finger. Then, in this state, the opening4 at the end of the protrusion portion 5 c is contacted with a sample.Then, in this state, the pressure applied to the chamber is released byweakening the force of pressing with a finger, so that the compressedportion of the covering can return to its original shape due to theelasticity of the covering. At this time, a suction pressure isdeveloped, and if the developed suction pressure is larger thanrequired, the sample is drawn in a manner, such as shown in FIG. 5. Thatis, because the liquid flow resistance (Z) in the drawing channel 2 abetween the branching portion of the bypass channel 6 and the analyticalsection 3 is the smallest among the three liquid stresses as describedabove, a sample 15 is first introduced into the opening 4 and furtherdrawn through the drawing channel 2 a into the analytical section 3 asshown in FIG. 5(A). If an excess of suction pressure still remains,because the liquid flow resistance (Y) in the bypass channel 6 a issmaller than the liquid flow resistance (X) in the drawing channel 2 b,an excess amount of the sample 15 and/or entrained air will flow intothe bypass channel 6 as shown in FIG. 5(B), and further part of them mayflow into the suction pressure generating chamber 1 as shown in FIG.5(C). At this time, because the liquid flow resistance (X) in thedrawing channel 2 b is the largest of the three, the sample introducedinto the analytical section 3 remains there, where a reaction between acomponent in the sample and a reagent (not shown) takes place togenerate a pigment, thereby developing a color in the reagent film. Inaddition, a possibility that the pigment might flow into the suctionpressure generating chamber 1 can be eliminated.

Furthermore, if an excess of suction pressure still remains, the excessamount of the sample 15 and/or entrained air present in the bypasschannel 6 is further discharged into the suction pressure generatingchamber 1 as shown in FIG. 5(D).

Then, the device in which a color is developed in the reagent film isset in a predetermined position in an optical measuring apparatus suchas a densitometer. Then, light is irradiated into the device, so thatwhen using the densitometer, reflected light is detected in a detectingsection to measure the developed color.

Thus, by having the bypass channel in the device and also providing saidrelationship of the liquid stresses in the three portion of thechannels, even if excess suction pressure is developed, the sample isensured to be introduced into the analytical section, where the sampleundergoes reaction with a reagent. Moreover, a possibility of overflowof the generated pigment can be eliminated. Accordingly, by using such adevice having a bypass channel, rapid sampling can be conducted withoutcarefully adjusting the force of pressing with a finger.

EXAMPLE 4

FIG. 6 shows an embodiment of a device for analyzing a sample of thepresent invention in which an analytical section is formed in the undersurface side of the body. In this device, light is irradiated from theunder surface side of the body. FIG. 6(A) is a plan view of such adevice, and FIG. 6(B) is a cross-sectional view of the device in FIG.6(A) taken along the line II—II.

As shown in the drawings, this device comprises an approximatelyrectangular plate shaped body 5, the body 5 comprising a base member 5 band a covering 5 a which covers over the surface of the base member.

In the upper surface of the base member 5 b, a suction pressuregenerating chamber 1 is formed in a portion on one end side of the body5 (left side in the drawings) relative to the center of the body 5, fromwhich a drawing channel 2 b extends toward the other end side of thebody. Then, the drawing channel 2 b extends downwards from the uppersurface side to the under surface side of the base member, where thechannel communicates with one end side of the analytical section 3formed in the under surface side of the base member 5 b. As shown in thedrawings, a reagent film 7 is disposed in the analytical section 3.Then, a drawing channel 2 a extends from the other end side of theanalytical section 3 to reach the upper surface side of the base member5 b, and then further extends toward the other end side of the body (theopposite side to the suction pressure generating chamber 1) in the uppersurface side of the base member 5 b, the end of the channel forming anopening 4. The opening 4 is formed into a funnel shape. Furthermore, abypass channel 6 also extends from the suction pressure generatingchamber 1, the end of the bypass channel merging into the drawingchannel 2 a between the analytical section 3 and the opening 4. Aportion of the bypass channel 6 from the merging portion is formed to bea bypass channel 6 a having a small diameter, while the whole drawingchannel 2 b has a small diameter, and the whole drawing channel 2 a hasa large diameter. As a result, the relationship of the liquid flowresistance (X) in the drawing channel 2 b, the liquid flow resistance(Y) in the bypass channel 6 a, and the liquid flow resistance (Z) in aportion of the drawing channel 2 a between the branching portion of thebypass channel 6 and the analytical section 3 is X>Y>Z.

In this device, the covering 5 a is not necessarily transparent,however, it may be transparent so that the process of drawing a samplecan be observed.

Furthermore, the materials of the base member 5 b and the covering 5 a,the dimensions of the suction pressure generating chamber, the drawingchannel, and the like in the device are the same as in the device of theembodiment previously described.

Next, an analysis using such a device is conducted, for example, asfollows.

First, a portion of the covering 5 a corresponding to the suctionpressure generating chamber 1 of the device is compressed by applying apressure, for example, by pressing with a finger. Then, in this state,the opening 4 is contacted with a sample.

Then, the pressure applied to the chamber is released by weakening theforce of pressing with a finger so that the compressed portion of thecovering 5 a can return to its original shape due to the elasticity ofthe covering. At this time, a suction pressure is generated, whereby thesample is drawn into the opening 4, and then further drawn through thedrawing channel 2 a into the analytical section 3. By having the bypasschannel 6 and providing the relationship of the three liquid flowresistances (X,Y,Z) of X>Y>Z in this device, even if excess suctionpressure is generated, the sample is ensured to be introduced into theanalytical section 3, where the sample undergoes reaction with areagent. In addition, a possibility that a generated pigment might flowinto the suction pressure generating chamber 1 can be eliminated. Then,the device in which a color is developed in the reagent film is set in apredetermined position in an optical measuring apparatus such as adensitometer. Then, light L is irradiated into the device from the undersurface side of the base member 5 b, so that when using thedensitometer, a reflected light is detected in a detecting section tomeasure the developed color.

EXAMPLE 5

Next, FIG. 7 shows a plan view of an embodiment of a device for multipleanalysis of the present invention. This device for multiple analysis iscapable of analyzing three items simultaneously.

As shown in the drawing, one end portion of the rectangular plate shapedbody 5 (the left end in the drawing) in this device is formed into aprotrusion portion 5 c, which is smaller than the body in width. Thewidth of the protrusion portion 5 c is decreasing toward the end.Furthermore, the body 5 comprises a base member and a covering whichcovers over the surface of the base member as in the predescribedembodiment.

In the upper surface of the base member, three drawing channels 2 bextend from a suction pressure generating chamber 1 formed in one endside portion of the body (right side in the drawing) relative to thecenter of the body. At each end of the respective drawing channels 2 bis formed an analytical section 3, different types of reagents (notshown) being disposed in the respective analytical sections 3, and threedrawing channels 2 a extend from the respective analytical sections 3,the ends of the respective drawing channels 2 a merging into one opening4. When the covering is transparent, the reagents are disposed bysticking reagent films on the inner surface of the coveringcorresponding to the respective analytical sections 3. A bypass channel6 extends from the suction pressure generating chamber 1, the end of thebypass channel merging into the opening 4. A certain portion of thebypass channel 6 from the merging portion is formed as a bypass channel6 a having a small diameter, while the whole drawing channels 2 b havesmall diameters, and the whole drawing channels 2 a have largediameters. As a result, the relationship of the liquid flow resistance(X) in the drawing channels 2 b, the liquid flow resistance (Y) in thebypass channel 6, and the liquid flow resistance (Z) in the portions ofthe drawing channels 2 a between the branching portion of the bypasschannel 6 and the analytical sections 3 is X>Y>Z.

In such a device for multiple analysis, the overall dimensions aredetermined as appropriate depending upon the number of the items to beanalyzed. Because three items are to be analyzed in this embodiment, thedimensions of the device are usually 20 to 50 mm in overall length, 20to 50 mm in width, and 1 to 5 mm in overall thickness, wherein theprotrusion portion is 10 to 20 mm in length, 5 to 20 mm in maximumwidth, 3 to 5 mm in minimum width. Other things such as materials,dimensions of the suction pressure generating chamber, the drawingchannels and the like, and so forth in-this device are the same as inthe device of prescribed embodiment having a bypass channel.Furthermore, the number of items to be analyzed is not particularlylimited, however, it is usually between 1 and 20, preferably between 3and 5. In this case, various number of analytical sections, bypasschannels and drawing channels may be formed depending upon the number ofthe items to be analyzed.

An analysis using such a device for multiple analysis may be performed,for example, as follows.

First, a portion of the covering 5 corresponding to the suction pressuregenerating chamber 1 of the device is compressed by applying a pressure,for example, by pressing with a finger.

Then, in this state, the opening 4 at the end of the protrusion portionis contacted with a sample. Then, the pressure applied to the chamber isreleased by weakening the force of pressing with a finger so that thecompressed portion of the covering can return to its original shape dueto the elasticity of the covering. At this time, a suction pressure isdeveloped, whereby the sample is drawn into the opening 4 and thenfurther drawn through the three drawing channels 2 a into the respectivethree analytical sections 3. By having the bypass channel 6 andproviding the relationship of the three liquid flow resistances (X,Y,Z)of X>Y>Z in this device, even if excess suction pressure is generated,the sample is ensured to be introduced into the analytical sections 3,where the sample undergoes reaction with a reagent, in addition, apossibility that a generated pigment might flow into the suctionpressure generating chamber 1 can be eliminated. Then, the device inwhich a color is developed in the reagent film is set in a predeterminedposition in an optical measuring apparatus such as a densitometer. Then,light is irradiated into the device, so that when using thedensitometer, a reflected light is detected in a detecting section tomeasure the developed color, so that three items can be analyzedsimultaneously.

EXAMPLE 6

FIG. 8 shows a plan view of an embodiment of a device for analyzing asample in which a portion of a drawing channel between an opening and abranching portion of a bypass channel snakes and also has a smalldiameter, so that the liquid stress in the portion of the drawingchannel becomes the largest.

As shown in the drawing, this device comprises an approximatelyrectangular plate shaped body 5 whose one end portion is decreasing inwidth toward the end, and the body 5 comprises a base member and acovering which covers over the surface of the base member.

Then, in the upper surface of the base member, a suction pressuregenerating chamber 1 is formed in a portion on the other end side (rightside in the drawing) relative to the center of the body 5, from which adrawing channel 2 b extends toward the one end portion of the bodyhaving decreasing width. An analytical section 3 is formed in a certainposition in the drawing channel 2 b (in an approximately center portionof the body 5). Then, a drawing channel 2 a extends from the analyticalsection 3 toward the portion of the body having decreasing width, andthe drawing channel 2 a snakes from a certain point. Furthermore, abypass channel 6 branches from the drawing channel 2 a, and it isbrought to be communicated with the suction pressure generating chamber1. Furthermore, as previously described, the drawing channel 2 a snakesfrom the branching portion of the bypass channel 6, and the end of thedrawing channel 2 a is formed into a funnel-shaped opening 4 on the endportion of the body having decreasing width. A reagent is disposed inthe analytical section 3, and when the covering is transparent, thereagent is disposed by sticking a reagent film containing the reagent ona portion of the inner surface of the covering corresponding to theanalytical section 3.

The whole portion of the drawing channel 2 a between the branchingportion of the bypass channel 6 and the analytical section 3 is made tohave a large diameter, and a portion 6 a of certain length from thebranching portion of the bypass channel 6 is made to have a smalldiameter, and the whole drawing channel 2 b is made to have a smalldiameter. The snaking portion of the drawing channel 2 a is made to havea small diameter and to be longer than the drawing channel 2 b. Thus,the liquid flow resistance (W) in the snaking portion of the drawingchannel 2 a is larger than the liquid flow resistance (X) in the drawingchannel 2 b. Accordingly, the relationship of the four liquid flowresistances, namely, the liquid flow resistance (W) in the snakingportion of the drawing channel 2 a, the liquid flow resistance (X) inthe drawing channel 2 b, the liquid flow resistance (Y) in the bypasschannel 6, and the liquid flow resistance (Z) in a portion of thedrawing channel 2 a between the branching portion of the bypass channel6 and the analytical section 3 is such that W>X>Y>Z.

In such a device, the snaking portion of the drawing channel 2 a isusually 5 to 15 mm in overall length, 0.1 to 0.5 mm in width, and 0.1 to0.5 mm in depth. Other things such as materials, the dimensions of thesuction pressure generating chamber and other portions of the drawingchannels, and the like are the same in this device as those in thepredescribed embodiment.

Next, an analysis using such a device is performed, for example, asfollows.

First, a portion of the covering 5 a corresponding to the suctionpressure generating chamber 1 of the device is compressed by applying apressure, for example, by pressing with a finger. Then, in this state,the opening 4 at the end of the protrusion portion is contacted with asample. Then, the pressure applied to the chamber is released byweakening the force of pressing with a finger, so that the compressedportion of the covering 5 a can return to its original shape due to theelasticity of the covering. At this time, a suction pressure isdeveloped, whereby a sample is drawn into the opening 4. Because therelationship of the four liquid flow resistances (W, X, Y, Z) isW>X>Y>Z, even if a strong suction pressure is developed, it is ensuredthat the sample is further introduced into the analytical section 3,where the sample is analyzed. Furthermore, because the liquid flowresistance (W) in the snaking portion of the drawing channel 2 a is thelargest, possibilities that the sample introduced into the analyticalsection 3 and/or a generated pigment might flow out toward the side ofthe opening 4 is reduced. Then, the device in which a color is developedin the reagent film is set in a predetermined position in an opticalmeasuring apparatus such as a densitometer. Then, light is irradiatedinto the device from the upper surface side of the body 5, so that whenusing the densitometer, a reflected light is detected in a detectingsection to measure the developed color.

EXAMPLE 7

FIG. 9 shows an embodiment of a device for analyzing a sample of thepresent invention. FIG. 9(A) is a plan view of such a device, and FIG.9(B) is a cross-sectional view of the device of FIG. 9(A) taken alongthe line III—III. As shown in the drawings, this device is formed bylamination of a plurality of films, and the body of the device is anapproximately rectangular plate shaped.

In this device, a suction pressure generating chamber 1 is formed as aprotrusion in a portion of one end side (right side in the drawings)relative to center of the approximately rectangular plate shaped body. Adrawing channel 2 extends from under side of the suction pressuregenerating chamber 1 toward the end opposite to the suction pressuregenerating chamber 1 (the other end) of the approximately rectangularplate shaped body. An analytical section 3 is formed in a certainposition in the drawing channel 2, and the end of the drawing channel 2communicates with the opening 4 formed in the other end of theapproximately rectangular plate shaped body through a liquid poolingportion 9. A window 10 is formed under the analytical section 3, if theneed arises. For example, if using glucose oxidase (GOD) as a reagent,because the reagent requires oxygen for coloring reaction, the windowshould be formed for supplying oxygen. However, except in such a case,when the portion of the film corresponding to the analytical section 3is transparent so that light can enter into the analytical section 3, itis not required to form the window. Furthermore, a reagent film 7impregnated with a reagent is disposed under the analytical section 3,so that it covers the window 10. Furthermore, a stopper which isgas-permeable and liquid-impermeable 8 is formed in a certain positionin the drawing channel 2 b between the suction pressure generatingchamber 1 and the analytical section 3 on the side of the suctionpressure generating chamber 1. The stopper 8 is formed by disposing ahydrophobic porous film in a certain position in the drawing channel 2b.

Furthermore, an air vent passage 25 branches from a portion of thedrawing channel 2 a between the liquid pooling portion 9 and theanalytical section 3, and the end 26 of the passage is open to theoutside of the body. By providing such an opening, capillarity can bedeveloped because of the air vent passage 25.

Furthermore, the area of the cross section of the air vent passage 25 ismade smaller than that of the cross section of the liquid poolingportion 9, so that the liquid flow resistance in the air vent passage 25is larger than that in the liquid pooling portion 9. Specifically, theliquid pooling portion 9 is about four times as wide as the drawingchannel 2 or the air vent passage 25, and the liquid pooling portion 9is about twice as thick as the drawing channel 2 or the air vent passage25.

Such a device of laminated films can be produced, for example, bylaminating films 11, 12, 13, and 14 formed into respective types ofshapes, with a reagent film 7 and a hydrophobic porous film 8 placedtherebetween, as shown in FIG. 10.

The film 14 is to be the under surface of the device, wherein the window10 is provided. In the film 13 are formed cutout portions to form theliquid pooling portion 9, the air vent passage 25, the analyticalsection 3, and the drawing channel 2, respectively. The film 12 ensuresthe thickness of the liquid pooling portion 9 (the size of thecross-sectional area of the portion). In the film 12 are formed acut-out portion in order to form the liquid pooling portion 9, acircular shaped cut-out portion in order to form an opening at the endof the air vent passage 25, and a circular shaped cut-out portion inorder to communicate the drawing channel 2 b with the suction pressuregenerating chamber 1. In the film 11 are formed a protrusion of anapproximately cylindrical convex portion in order to form the. suctionpressure generating chamber 1 and a circular cut-out portion in order toform an opening at the end of the air vent passage 25.

Then, the reagent film 7 is disposed in a portion between the film 14and the film 13 where the analytical section 3 is to be formed, and thehydrophobic porous film 8 is disposed between the film 13 and the film12 in a portion to be a part of the drawing channel 2 b. In this state,the four films 14, 13, 12, and 11 are laminated in this order from thebottom and then integrated together to produce a device as shown in FIG.9.

An example of the hydrophobic porous film is a hydrophobic resin porousfilm, specifically, a polyethylene porous film, a polypropylene porousfilm, a Teflon porous film, or the like. Suitable hydrophobic resinporous films are Celgard (Product Name/Hoechst Celanese Co., Ltd.), andHipore (Product Name/Asahi Chemical Industry Co., Ltd.). The averagediameter of a pore in the hydrophobic resin porous film is usually from0.1 to 1 μm, preferably from 0.3 to 0.7 μm. Furthermore, the thicknessof the hydrophobic resin porous film is usually from 10 to 100 μm. Sucha hydrophobic resin porous film can be produced, for example, by forminga film using said hydrophobic resin and then orienting the film eitheruniaxially or biaxially.

The reagent film 7 is a film impregnated with a reagent, and the type ofthe reagent is selected as appropriate depending upon the type of theobject for analysis. The structure of the reagent film is alsodetermined as appropriate depending upon the type of the object to beanalyzed. For example, when plasma components of blood is the object foranalysis, the reagent film usually has a structure in which a filtrationlayer for separating blood cells, a reagent layer impregnated with areagent, and a base member are laminated in this order. Then, thereagent film 7 is arranged in the analytical section 3 so that thefiltration layer can contact with blood (a liquid sample). Moreover,conventionally known materials can be applies for the respective layersin the reagent film.

When producing a device of the present invention, the films may beintegrated by using an adhesive to bond the respective films to eachother or by laminating the films by pressing or heating.

Furthermore, suitable materials for the films which comprise the deviceare, for example, polyethylene, polyethylene terephthalate (PET),polystyrene, polyvinyl chloride, and the like, and particularly PET isdesired because of processability.

The dimensions of the device shown in FIG. 9 are usually 15 to 60 mm inlength, 5 to 20 mm in width, and 1 to 3 mm in thickness. Furthermore,the dimensions of the suction pressure generating chamber 1 are usually3 to 15 mm in diameter and 0.5 to 3 mm in height. Furthermore, thedimensions of the drawing channel 2 are usually 10 to 40 mm in overalllength, 0.5 to 2 mm in width, and 0.1 to 0.5 in thickness, wherein thedrawing channel 2 a is 5 to 30 mm in length, and the drawing channel 2 bis 5 to 30 mm in length. Furthermore, the dimensions of the analyticalsection 3 are usually 2 to 10 mm in diameter and 0.1 to 1 mm in height.The dimensions of the liquid pooling portion 9 are usually 2 to 10 mm inlength, 2 to 10 mm in width, and 0.2 to 1 mm in thickness. Thedimensions of the air vent passage 25 are usually 2 to 10 mm in overalllength, 0.5 to 2 mm in width, 0.1 to 0.5 mm in thickness, and 0.5 to 5mm in diameter of the opening of the passage. The dimensions of theopening 4 are usually 2 to 10 mm in width and 0.2 to 1 mm in thickness.

Next, a method for analyzing a sample using the device shown in FIG. 9will be described by referring to FIG. 11. In FIG. 11, the same parts asshown in FIG. 9 are referred to by using the same signs.

First, the protruding suction pressure generating chamber 1 in thedevice is compressed by applying pressure, for example, by pressing witha finger. Then, in this state, the opening 4 is contacted with a sample15 in a predetermined sampling spot. Then, as shown in FIG. 11(A), thesample 15 is drawn by capillarity developed due to the air vent passage25 into the opening 4 and retained in the liquid pooling portion 9.Then, the opening 4 is detached from the sampling spot, and then theforce of pressing with a finger is weakened to release the appliedpressure. Then, the compressed suction pressure generating chamber 1returns to the original shape due to the elasticity, whereby a suctionpressure (a negative pressure) is developed. Due to the developedsuction pressure, the sample is retained in the liquid pooling portion 9is drawn through the drawing channel 2 a into the analytical section 3as shown in FIG. 11(B). The time period required for introducing thesample into the analytical section 3 in such a method is markedly shortcompared to the time required for drawing a sample by using capillarity.In addition, such a drawing process is hardly affected by properties ofthe sample such as viscosity. Furthermore, in this drawing process,because the liquid stresses in the liquid pooling portion 9 and the airvent passage 25 are adjusted as described above, a part of the sample 15remains in the air vent passage 25 as shown in the drawing, so that airinclusion can be prevented. Furthermore, even if excess suction pressureis developed, because the stopper 8 is formed, it is ensured that thesample 15 is introduced into the analytical section 3 without causing aflow of the sample 15 into the suction pressure generating chamber 1.Accordingly, it is not necessary to take care in adjusting the pressingforce with a finger. Then, in the analytical section 3, a reactionbetween a component in the sample 15 and the reagent contained in thereagent film 7 takes place to generate a pigment, whereby a color isdeveloped in the reagent film 7. Then, the device in which a color isdeveloped in the reagent film 7 is set in a predetermined position in anoptical measuring apparatus such as a densitometer. Then, light isirradiated into the device through the window 10 formed in the undersurface of the device, so that when using the densitometer, a reflectedlight is detected in a detecting section to measure the color developedthe regent film. Furthermore, in this measuring, when both the wholeanalytical section 3 and the reagent film 7 are transparent, analysiscan also be conducted by using a transmitted light.

EXAMPLE 8

FIG. 12 shows a plan view of an embodiment of a device for multipleanalysis provided with a plurality of analytical sections arranged inseries.

As shown in the drawing, this device is provided with three analyticalsections 3 in certain positions in a drawing channel 2, and a reagentfilm 7 is disposed in each of the analytical sections 3. The respectivereagent films 7 are impregnated with different types of reagents. Thestructure of the device other than these aspects is the same as that ofthe device shown in FIG. 9, and the same parts as in FIG. 9 are referredto by using the same signs.

This device can be produced by laminating a plurality of films havingpredetermined shapes and then integrating them together, as in thepredescribed device in Example 7, and the method for producing thedevice, used materials, and the like are also the same as in the devicein Example 7. Furthermore, the overall dimensions of the device areusually 15 to 100 mm in length, 5 to 20 mm in width, and 1 to 3 mm inthickness. Furthermore, the whole length of the drawing channel 2 isusually 20 to 80 mm, and the spacing between the analytical sections isusually 3 to 10 mm. The dimensions in other parts of the device are thesame as in the device of Example 7.

Although a device provided with three analytical sections is describedin this embodiment, the present invention is not limited to such adevice, and any number of analytical sections can be provided dependingupon the desired number of items for measurement.

Next, a method for analysis using such a device for multiple analysis isperformed, for example, as follows.

First, a suction pressure generating chamber 1 of the device iscompressed by pressing as in the predescribed embodiment. Then, in thisstate, the opening 4 is contacted with a sample in a predeterminedsampling spot, whereby the sample is drawn by capillarity into theliquid pooling portion 9 where it is retained. Then, the opening 4 isdetached from the sampling spot, and thereafter the pressure applied tothe suction pressure generating chamber 1 is released, so that a suctionpressure is developed. Accordingly, the sample is introduced into therespective three analytical sections 3 one after another, whererespective reactions between compounds in the sample and the reagentscontained in the respective reagent films 7 take place. Then, the deviceis set in a predetermined position in an optical measuring apparatuscapable of performing multiple analysis. Then, light is irradiatedthrough the window formed in the under surface of the device, wherebythe colors developed in the respective reagent films 7 are measured. Anexample of the optical measuring apparatus is a densitometer. Thus, byusing such a device for multiple analysis, a plurality of items can bemeasured simultaneously.

EXAMPLE 9

FIG. 13 shows a plan view of a device for analyzing a sample formultiple analysis provided with a plurality of analytical sectionsarranged in parallel.

As shown in the drawing, this device has three drawing channels 2. Ananalytical section 3 is formed in each of the drawing channels 2, wherea reagent film 7 is disposed. Each reagent film 7 is impregnated with atype of reagent different to each other. The portions of each of thethree respective drawing channels 2 which extend from the threerespective analytical sections 3 toward the opening 4 merge to form adrawing channel 2 a in a certain position before reaching the liquidpooling portion 9. Furthermore, three drawing channels 2 b extend from asuction pressure generating chamber 1 and are in communication with thethree analytical sections 3, respectively. This device and the deviceshown in FIG. 9 in Example 7 have the same structure other than thesecharacteristics, therefore, the same parts are referred to by using thesame signs.

This device can be produced by laminating a plurality of films havingpredetermined shapes and then integrating them together, as in thepredescribed device in Example 7, and the method for producing thedevice, the materials used, and the like are also the same as those inExample 1. Furthermore, the overall dimensions of the device are usually15 to 60 mm in length, 10 to 50 mm in width, 1 to 3 mm in thickness.Furthermore, the overall length of the drawing channel 2 is usually 10to 40 mm, and the spacing of the analytical sections 3 to each other isusually 3 to 10 mm. The dimensions of other parts of the device are thesame as in the device of Example 7.

Although a device provided with three analytical sections is shown inthis embodiment, the present invention is not limited to this device,and any number of analytical sections and drawing channels can beprovided depending upon the desired number of items for measurement.

Next, an analysis using such a device for multiple analysis isperformed, for example, as follows.

First, a suction pressure generating chamber 1 of the device iscompressed by pressing as in the predescribed embodiment. In this state,the opening 4 is contacted with a sample in a predetermined samplingspot, and the sample is introduced by capillarity into the liquidpooling portion 9, where it is retained. Then, the opening 4 is detachedfrom the sampling spot, and thereafter the pressure applied to thesuction pressure generating chamber 1 is released so that a suctionpressure is developed. As a result, the sample is introduced into eachof the three analytical sections 3 simultaneously, where reactionsbetween components in the sample and the reagents contained in therespective reagent films 7 take place. Then, the device is set in apredetermined position in an optical measuring apparatus capable ofperforming multiple analysis. Then, light is irradiated through thewindow formed in the under surface of the device, whereby the colordeveloped in the respective reagent films 7 is measured. Thus, by usingsuch a device for multiple analysis, a plurality of items can bemeasured simultaneously. An example of the optical measuring apparatusis a densitometer.

Having described the devices for multiple analysis in Example 8 andExample 9, whether the analytical sections are arranged either in seriesor in parallel may be determined by various conditions such as influenceof the reagents to each other, the shapes of the device, or the like.

EXAMPLE 10

FIG. 14 shows a plan view of a device for analyzing a sample in which areagent positioning section, reagent reaction section, and a measuringsection are provided independently in certain positions in the drawingchannel.

As shown in the drawing, this device is provided with a reagentpositioning section 32, a reagent reaction section 30, and a measuringsection 31, each of them being formed in a certain position in a drawingchannel 2. The shape of the drawing channel does not particularly changedue to the reagent positioning section 32, and a reagent is simplydisposed in the drawing channel. Also, it may be a depressed cylindricalshaped cavity like the reagent reaction section. Moreover, the reagentcan be disposed by simply positioning the reagent in the channel. orattaching the reagent to the reagent positioning section by using ahydrophilic polymer or the like. Examples of the reagents includewet-type reagents or the like capable of moving together with a sample.More particularly, example of such reagents are, GOD, peroxidase (POD),4-aminoantipyrine, N-ethyl-N-(2-hydroxyne-3-sulfopropyl)-3-methylaniline(TOOS) and the like. Moreover, even a dry-type reagent can move togetherwith a sample if it can be dissolved in a sample. Furthermore, thereagent reaction section 30 is formed in a same way as in thepredescribed embodiment other than that a reagent film is not disposedtherein. Furthermore, the measuring section 31 is formed into adepressed cylindrical shaped cavity like the reagent reaction section30, except that it is made transparent for permitting light entrance.Moreover, an absorbent member such as a filter paper may be disposed inthe measuring section 31 in order to fix the transferred pigment. Thisdevice and the device shown in FIG. 9 in Example 7 have the samestructure other than these characteristics, therefore the same parts arereferred to by using the same signs. Moreover, the reagent reactionsection 30 may also serve as a measuring section like in Example 7, andin such a case, the reagent reaction section 30 is made transparent forpermitting light entrance.

This device for analyzing a sample can be produced by laminating aplurality of films having predetermined shapes and then integrating themtogether, as in the predescribed embodiment in Example 7. In addition,the method for producing such a device, the materials used, and the likeare also the same as those in Example 7. Furthermore, generally areagent is prepositioned by using a hydrophilic polymer or the likeduring lamination process of the films. Furthermore, the overalldimensions of the device are usually 15 to 100 mm in length, 5 to 20 mmin width, and 1 to 3 mm in thickness. Furthermore, the overall length ofthe drawing channel 2 is usually 20 to 80 mm, and the spacing betweenthe reagent positioning section, the reagent reaction section 30, andthe measuring section 31 to each other is usually 3 to 10 mm. Thedimensions of other parts of the device are the same as in theembodiment in Example 7.

Next, an analysis using such a device for multiple analysis isperformed, for example, as follows.

First, a suction pressure generating chamber 1 is compressed by pressingas in the predescribed embodiment. In this state, the opening 4 iscontacted with a sample in a predetermined sampling spot, and the sampleis drawn by capillarity into the liquid pooling portion 9, where it isretained. Then, the opening 4 is detached from the sampling spot, andthereafter the pressure applied to the suction pressure generatingchamber 1 is released so that a suction pressure is developed. As aresult, the sample is transferred into the reagent positioning section32, into the reagent reaction section 30, and then into the measuringsection 31 in this order. Then, the sample first moves into the reagentreaction section 30 with the reagent present in the reagent positioningsection 32, where a reaction between a component in the sample and thereagent takes place to generate a pigment. The pigment may be producedin a portion between the reagent reaction section 30 and the measuringsection 31. Then, the pigment moves to the measuring section 31. If afilter paper is positioned in the measuring section 31, a color isdeveloped in the filter paper. Then, the device is set in apredetermined position in an optical measuring apparatus. Then, light isirradiated into the measuring section, whereby the color of the pigmentor the color developed in the filter paper is measured by using anoptical measuring apparatus such as a densitometer. As a condition ofthis measurement, when using the predescribed reagents such as GOD, thismeasuring should be performed one minute after the reaction with awavelength of 570 nm.

EXAMPLE 11

FIG. 15 shows a plan view of a device for analyzing a sample in whichtwo reagent positioning sections are provided in certain positions inthe drawing channel.

As shown in the drawing, this device is provided with a first reagentpositioning section 32 a and a second reagent positioning section 32 bformed in certain positions in a drawing channel 2, the two sectionsforming the reagent reaction section 30, and further provided with ameasuring section 31. Usually, a first reagent is disposed in the firstreagent positioning section 32 a, and a second reagent is disposed inthe second reagent positioning section 32 b.

Although the first reagent positioning section 32 a and the secondreagent positioning section 32 b are formed into depressed cylindricalshaped cavities, reagents may be simply disposed in the drawing channel2 without changing the shape of the channel, as described later.Furthermore, in disposing the reagents, the reagents may be attached tothe reagent positioning sections by using a hydrophilic polymer or thelike, while it may be simply positioned as in the predescribed device inExample 10. Suitable reagents are those comprising two or morecomponents which cannot be mixed prior to a reaction with a sample, aspreviously described. An example of such a reagent is anenzyme-substrate type reagent, specifically, trypsin-substrate typereagent. The substrate usually generates a pigment through an enzymereaction.

Furthermore, when dissolved and mixed in a sample, this reagent iscapable of moving.

Also, the measuring section 31 is formed as a depressed cylindricalshaped cavity like the reagent positioning section. Further, anabsorbent member such as a filter paper may be disposed in the measuringsection 31 in order to fix the transferred pigment. This device and thedevice shown in FIG. 9 in Example 7 have the same structure other thanthese characteristics, therefore, the same parts are referred to byusing the same signs. Moreover, a reagent reaction section may serve asa measuring section like in Example 7. In case of this embodiment, thesecond positioning disposed section 32 b may serve as the measuringsection 31.

This device can be produced by laminating a plurality of films havingpredetermined shapes and then integrating them together, as in thepredescribed device in Example 7. In addition, the method for producingsuch a device, the materials used, and the like in this device are alsothe same as those in Example 7. Furthermore, generally a reagent isprepositioned by using a hydrophilic polymer or the like duringlamination process of the films. Furthermore, the overall dimensions ofthe device are usually 15 to 100 mm in length, 5 to 20 mm in width, and1 to 3 mm in thickness. Furthermore, the overall length of the drawingchannel 2 is usually 20 to 80 mm, and the spacing between the reagentpositioning sections and the measuring section is usually 3 to 10 mm.The dimensions of other parts of the device are the same as in Example7.

Next, an analysis using this device is performed, for example, asfollows.

First, as in the predescribed embodiment, a suction pressure generatingchamber 1 is compressed by applying pressure. In this state, the opening4 is contacted with a sample in a predetermined sampling spot, and thesample is drawn by capillarity into the liquid pooling portion 9 to beretained. Then, the opening 4 is detached from the sampling spot, andthen the pressure applied to the suction pressure generating chamber 1.is released so that a suction pressure is developed. As a result, thesample is transferred into the first reagent positioning section 32 a,into the second reagent positioning section 32 b, and into the measuringsection 31 in this order. Then, the sample first moves into the secondreagent positioning section 32 b with the first reagent present in thefirst reagent disposed section 32 a, where the three of the sample, thefirst reagent, and the second reagent are reacted to each other togenerate a pigment. The pigment may be generated in a portion betweenthe second reagent disposed section 32 b and the measuring section 31.Then, the pigment moves to the measuring section 31 When a filter paperis positioned in the measuring section 31, a color is developed in thefilter paper. Then, the device is set in a predetermined position in anoptical measuring apparatus. Then, light is irradiated into themeasuring section 31, whereby the color of the pigment or the colordeveloped in the filter paper is measured by using an optical measuringapparatus such as a densitometer.

EXAMPLE 12

FIG. 16 shows a plan view of a device for analyzing a sample in whichthree reagent positioning sections and a measuring section are providedin certain positions in a drawing channel. This device has a structurein which those in Example 10 and 11 are integrated.

As shown in the drawing, this device is provided with a first reagentpositioning section 32 a, a second reagent positioning section 32 b, anda third reagent positioning section 32 c formed in certain positions ina drawing channel 2, all of these forming a reagent reaction section 30in combination, and further provided with a measuring section 31 formedin a certain position in-the drawing channel 2. Usually, a first-reagentis disposed in the first reagent positioning section 32 a, a secondreagent is disposed in the second reagent positioning section 32 b, anda third reagent is disposed in the third reagent positioning section 32c.

The reagents are simply disposed in the respective three reagentpositioning sections 32 a, 32 b, and 32 c without changing the shape ofthe drawing channel 2. Furthermore, in disposing the reagents, they maybe simply disposed in the drawing channel as in the device previouslydescribed in Example 4, or alternatively, the reagents may be attachedto the respective reagent positioning sections by using a hydrophilicpolymer or the like. Suitable reagents are those comprising two or morecomponents which cannot be mixed prior to a reaction with a sample aspreviously described. Examples of such a reagent includeenzyme-substrate type reagents, for example, a reagent comprising atrypsin, the substrate of the trypsin, and a buffer solution. By usingsuch a reagent, for example, a trypsin inhibitor in urine can bemeasured. Furthermore, a pigment is generated through a reaction betweenthe substrate and the enzyme. With regard to this reagent, the firstreagent is the buffer solution, the second reagent is the trypsin, andthe third reagent is the substrate. Besides, when dissolved and mixed ina sample, this reagent is capable of moving.

The measuring section 31 is formed as a depressed cylindrical shapedcavity. An absorbent member such as a filter paper may be disposed inthe measuring section 31 in order to fix the transferred pigment. Thestructure of this device other than these characteristics is the same asthat of the device shown in FIG. 9 in Example 7, therefore the sameparts are referred to by using the same signs.

This device can be produced by laminating a plurality of films havingpredetermined shapes and then integrating the films together, as in thedevice described in Example 7. In addition, the method for producingsuch a device, the materials used, and the like are also the same asthose in Example 7. Furthermore, the reagents are generally disposed inadvance by using hydrophilic polymers or the like during the process oflaminating the films. Furthermore, the overall dimensions of the deviceare usually 15 to 100 mm in length, 5 to 20 mm in width, and 1 to 3 mmin thickness. Furthermore, the whole length of the drawing channel 2 isusually 20 to 80 mm, and the spacing between the reagent positioningsections and the measuring section is usually 3 to 10 mm. The dimensionsof other parts of the device are the same as in Example 7.

Next, a method for analyzing a sample by using this device will bedescribed by referring to a case using the predescribed reagentcomprising a buffer solution, a trypsin and a substrate.

First, the device for analyzing a sample having a buffer solution in thefirst reagent positioning section 32 a, a trypsin in the second reagentpositioning section 32 b, and a substrate in the third reagentpositioning section 32 c is prepared. Then, as in the predescribedembodiment, a suction pressure generating chamber 1 is compressed byapplying a pressure, and in this state, the opening 4 is contacted witha sample (urine) in a predetermined sampling spot, so that the sample isdrawn by capillarity into the liquid pooling portion S to be retained.Then, the opening 4 is detached from the sampling spot, and then thepressure applied to the suction pressure generating chamber 1 isreleased so that a suction pressure is developed. As a result, thesample is transferred into the first reagent positioning section 32 a,into the second reagent positioning section 32 b, into the third reagentpositioning section 32 c, and into the measuring section 31 in thisorder. Then, the sample moves into the second reagent positioningsection 32 b with the buffer solution present in the first reagentpositioning section 32 a, where the sample, the buffer solution, and thetrypsin are mixed together. Then, the mixture is transferred into thethird reagent positioning section 32 c, where it is mixed with thesubstrate, whereby an enzyme reaction is caused to generate a pigment.Moreover, the pigment may be generated in a position between the thirdreagent positioning section 32 c and the measuring section 31. Then, thepigment moves to the measuring section 31. Therefore, when a filterpaper is positioned in the measuring section 31, a color is developed inthe filter paper. Then, the device is set in a predetermined position inan optical measuring apparatus. Then, light is irradiated into themeasuring section 31, whereby the color of the pigment or the colordeveloped in the filter paper is measured by using an optical measuringapparatus such as a densitometer.

EXAMPLE 13

Next, an embodiment of a device for analyzing a sample of the presentinvention in which a vent is formed in a suction pressure generatingchamber will be described.

FIG. 17 shows a cross-sectional view of an embodiment of this device. Asshown in FIG. 17(A), the basic structure of the device is the same asthat of the device shown in FIG. 9 in Example 7, and the same parts arereferred to by using the same signs. The vent 1 a is usually 0.1 to 5 mmin diameter. An analysis of a sample by using this device is conducted,for example, as follows.

First, the opening 4 of the device is contacted with a sample, so thatthe sample 15 is retained in the liquid pooling portion 9. Then, asshown in FIG. 17(B), the suction pressure generating chamber 1 ispressed with a finger or the like. At this time, because the air in thesuction pressure generating chamber 1 is discharged through the vent 1a, the sample is not discharged through the opening 4 by the air forcedfrom the suction pressure generating chamber 1. Then, as shown in FIG.17(C), the vent 1 a is closed with a finger or the like when the suctionpressure generating chamber 1 is compressed. Then, when the pressureapplied to the suction pressure generating chamber 1 is released in astate in which the vent 1 a is closed as shown in FIG. 17(D), thesuction pressure generating chamber 1 returns to its original shape andthereby a suction pressure is developed. As a result, the sample 15 istransferred through the drawing channel 2 into the analytical section 3.The subsequent analyzing operation is the same as in Example 7.

Accordingly, by using such a device in which the suction pressuregenerating chamber 1 is provided with the vent 1 a, it is possible toapply a pressure to the suction pressure generating chamber 1 after theopening 4 is contacted with the sample 15 and the sample is retained inthe liquid pooling portion. As a result, sampling can be performedeasily.

EXAMPLE 14

Next, an embodiment of a device of the present invention in which asuction pressure generating tube is used as a suction pressuregenerating means will be described.

FIG. 18 shows a cross-sectional view of an embodiment of such a devicefor analyzing a sample. As shown in FIG. 18(A), this device has the samestructure as that of the device shown in FIG. 9 in Example 7, exceptthat a suction pressure generating tube 21 is provided in place of asuction pressure generating chamber, and the same parts are referred toby using the same signs. The suction pressure generating tube 21 can beformed, for example, by placing a resin sheet, which is bent so that theshape of a cross-section of the sheet in longitudinal direction becomesapproximately a reverse U-shaped, on the body of the device. In thiscase, one end of the suction pressure generating tube communicatesthrough a stopper 8 which is gas-permeable and liquid-impermeable withthe drawing channel 2, and the other end is closed. In the suctionpressure generating tube, usually the sheet is 0.01 to 2 mm inthickness, and the tube is 0.5 to 5 mm in height on the inside, 1 to 10mm in width on the inside, and 5 to 30 mm in length. It is desired thatthe suction pressure generating tube 21 is formed so that it may notoverlap with the drawing channel 2, an analytical section 3, or thelike. This because it is necessary to compress the tube by applying apressure through a hand in order to develop a suction pressure by thesuction pressure generating tube 21, and there is a possibility that theshape of the drawing channel or the like might be changed by thepressure. Suitable materials for the resin sheet are, for example, softvinyl chloride resin, soft silicon resin, natural rubber, and the like.Furthermore, the shape of a cross section of the suction pressuregenerating tube in a longitudinal direction is not limited to saidreverse U-shape. For example, it may be rectangular or the like.

A sample may be analyzed by using this device, for example, as in thefollowing steps. First, the opening 4 of the device is contacted with asample, so that the sample 15 is retained in a liquid pooling portion 9.Then, as shown in FIG. 18(B), a portion of the suction pressuregenerating tube 21 on one end side (right end in the drawings) incommunication with the drawing channel 2 is pressed with a finger or thelike, whereby the corresponding portions of the sheet are adhered toeach other. Then, as shown in FIG. 18(C) and FIG. 18(D) successively,the tube can be drawn by moving the pressing portion toward the openend. As a result, a suction pressure is developed in the suctionpressure generating tube 21, whereby the sample 15 is moved through thedrawing channel 2 into the analytical section 3. Subsequent analyzingoperation is conducted in the same way as in Example 7.

Accordingly, by using such a device having the suction pressuregenerating tube as the suction pressure generating means, a suckingoperation can be performed after the opening 4 is contacted with thesample 15, which is then retained in the liquid pooling portion, as inthe device provided with a suction pressure generating chamber havingthe vent 1 a. As a result, sampling can be operated more easily.

EXAMPLE 15

Next, an embodiment of the present invention where a sample is analyzedby an electrochemical means will be described.

FIG. 19 shows a device for analyzing a sample provided with electrodes.FIG. 19(A) is a plan view of the device, and FIG. 19(B) is across-sectional view of the device shown in FIG. 19 (A) taken along theline IV—IV . The device shown in these drawings has the same structureas the device in Example 7, except that the electrodes are formed and nowindow is formed, therefore the same parts are referred to by using thesame signs.

As shown in the drawings, the electrodes comprise a working electrode 33a and a counter electrode 33 b, which are formed under the analyticalsection 3. Both of the electrodes extend beyond the suction pressuregenerating chamber 1, and the ends of them are formed into terminals 33c and 33 d, respectively.

This device can be produced by laminating the films formed intorespective predetermined shapes as in Example 7. For example, as shownin FIG. 20, the device can be produced by laiminating films 11, 12, 13,and 14 formed into respective type of shapes, with a reagent film 7 anda hydrophobic porous film 8 positioned therebetween.

The film 14 forms the under side portion of the device, and theelectrodes (33 a, 33 b, 33 c, 33 d) are formed on the upper surface ofthe film. The electrodes can be formed, for example by printing theterminals (33 c and 33 d) on the film by screen printing using silver(Ag) paste, while printing the working electrode 33 a and the counterelectrode 33 b by screen printing using conductive carbon paste. Thedimensions of the electrodes are, for example, in case of the shapeshown in the drawing, usually 1 to 14 mm in outer diameter of theworking electrode 33 a, 3 to 15 mm in outer diameter of the counterelectrode 33 b, and 0.5 to 2 mm in width of the spacing between theseelectrodes Furthermore, the overall length of the electrode includingthe terminals is 10 to 50 mm. Moreover, the shapes of the electrodes arenot limited to the shapes shown in the drawing. The material for thefilm is not particularly limited as long as it has insulating property,and for example, PET, polypropylene, polyester or the like may be used.Furthermore, a hole to form a window is not formed in the film 14.Furthermore, the film 14 is not necessarily transparent, and it may becolored.

In producing this device, a reagent film 7 produced independently may beused, or alternatively, the reagent film 7 may be directly formed on theelectrodes (the working electrode and the counter electrode). Forexample, the reagent film can be formed by applying a hydrophilic highpolymer aqueous solution on the electrodes portion followed by drying,thereupon further applying a reagent solution followed by drying. Anexample of the high polymer aqueous solution is a 0.5% by weight aqueoussolution of carboxymethyl cellulose. In case of analyzing lactic acid,for example, a suitable reagent solution is 400 U/ml of lactate oxidaseand 2.0% by weight aqueous solution of potassium ferricyanide.Furthermore, in case of analyzing glucose, glucose oxidase may be usedin place of said lactate oxidase, and in case of analyzing cholesterol,cholesterol oxidase may be used in place of said lactate oxidase.

Next, a method for analyzing a sample by using this device will bedescribed. First, as in the predescribed embodiments, the suctionpressure generating chamber 1 is compressed, and in this state, theopening 4 is contacted with a sample in a predetermined sampling spot,thereby the sample is drawn by capillarity into the liquid poolingportion 9 to be retained. Then, the pressure applied to the suctionpressure generating chamber 1 is released to develop a suction pressure,whereby the sample is moved into the reagent film 7 positioned in theanalytical section 3, where a reaction with the reagent takes place.Then, the device is set in a predetermined position in anelectrochemical measuring apparatus, and after a reaction of apredetermined time period, a certain amount of voltage is appliedbetween the working electrode and the counter electrode, and the flowingelectric current is measured.

EXAMPLE 16

Next, an embodiment of the present invention in which a device of thepresent invention is used in an analysis using immunoassay will bedescribed.

FIG. 21(A) shows a plan view of a device for analyzing a sample forimmunoassay. As shown in the drawing, in this device, a liquid poolingportion 9 a is formed as a depressed cylindrical shaped cavity, and acircular opening 4 a is formed thereon. Furthermore, four analyticalsections 3 a, 3 b, 3 c, and 3 d are formed in certain positions in thedrawing channel 2. A reagent film 7 a containing an antibody, which islabelled by a colored material such as gold colloid through reactionwith a target antigen in a sample (a labelled antibody), is disposed inthe analytical section 3 a. Furthermore, a reagent film 7 b, where anantibody which reacts with the same antigen mentioned above isimmobilized, is disposed in the analytical section 3 b. Furthermore, arinsing solution 16 is disposed in the analytical section 3 d. The restof the structure is the same as in the device shown in FIG. 9 in Example7, therefore the same parts are referred to by using the same signs.

Immunoassay using this device is performed, for example, as shown inFIG. 21(B)-(H). First, the suction pressure generating chamber 1 iscompressed by pressing, and in this state, the opening 4 a is contactedwith a sample, whereby the sample is drawn by capillarity into theliquid pooling portion 9 a to be retained (FIG. 21(B)). At this time,the rinsing solution 16 is forced to move into the analytical section 3b by the air discharged from the suction pressure generating chamber.Then, the pressing force applied to the suction pressure generatingchamber 1 is slightly weakened to develop a weak suction pressure,thereby the sample is moved into the analytical section 3 a, where areaction between the antigen in the sample and the labelled antibodytakes place (FIG. 21(C)). At this time, the rinsing solution is movedinto the analytical section 3 c by the suction pressure. Then, when thepressure applied to the suction pressure generating chamber 1 iscompletely released to develop a suction pressure, the sample is movedinto the analytical section 3 b, where the antigen in the sample isreacted with the immobilized antibody (FIG. 21(D)). Furthermore, at thistime, the rinsing solution 16 is moved into the analytical section 3 d.Then, the suction pressure generating chamber 1 is lightly compressedagain, and the resulting discharged air forces the sample to move intothe analytical section 3 a (FIG. 21(E)). Then, the antigens linked tothe immobilized antibodies remain in the analytical section 3 b, theantigen being labelled by the labelled antibodies. However, a number oflabelled antibodies which are not linked to the antigens also remain inthe analytical section 3 b. At this time, the rinsing solution 16 istransferred into the analytical section 3 c. Then, the suction pressuregenerating chamber 1 is further strongly compressed so that the sampleis moved into the liquid pooling portion 9 a forced by the dischargedair, and also the rinsing solution 16 moved into the analytical section3 b (FIG. 21(F)). Then, the pressure applied to the suction pressuregenerating chamber 1 is slightly released to generate a weak suctionpressure, whereby the rinsing solution 16 is moved to the analyticalsection 3 c (FIG. 21(G)). As a result, the analytical section 3 b isrinsed, and only the antigens linked both to the immobilized antibodiesand to the labelled antibodies are present in the analytical section 3b. At this time, the sample is transferred into the analytical section 3a. Then, in this state, the amount of the labelled antibodies present inthe analytical section Sc is measured by using an optical means. Aftermeasuring, the pressure applied to the suction pressure generatingchamber 1 is completely released (FIG. 21(H)), and the device isdiscarded.

Finally, it is to be understood that the invention may be embodied inother specific forms without departing from the spirit or essentialcharacteristics thereof. The embodiments disclosed in this applicationare to be considered in all respects as illustrative and notrestrictive, so that the scope of the invention being indicated by theappended claims rather than by the foregoing description, and allchanges which come within the meaning and range of equivalency of theclaims are intended to be embraces therein.

What is claimed is:
 1. A device for collecting a sample for analysis,comprising: a main body; a suction pressure generator; a drawing channelformed in the main body in communication with the suction pressuregenerator, an opening in the main body being formed at the end of saiddrawing channel distal with respect to said suction pressure generator;and an analytical section formed in said drawing channel between thesuction generator and the opening, the analytical section communicatingdirectly with the exterior of the device through the drawing channel,wherein a gas-permeable and liquid-impermeable stopper is provided inthe drawing channel between the suction pressure generator and theanalytical section and in use a sample is drawn into the main bodythrough the opening by suction pressure developed by said suctionpressure generator, and then the sample is transferred by the suctionpressure through the drawing channel into the analytical section.
 2. Adevice as claimed in claim 1, wherein a plurality of analytical sectionsare formed in the drawing channel, and the stopper is provided in thedrawing channel between said suction pressure generating means and theanalytical section closest to the suction pressure generating means. 3.A device as claimed in claim 1, wherein the opening has a shapeenlarging toward the end.
 4. A device as claimed in claim 1, wherein theanalytical section formed in the drawing channel serves as a reagentpositioning section and a reagent reaction section.
 5. A device asclaimed in claim 1, wherein the suction pressure generator means is asuction pressure generating tube.
 6. A device as claimed in claim 1,wherein a pair of electrodes comprising a working electrode and acounter electrode is provided in at least one analytical section.
 7. Adevice as claims in claim 1, wherein the drawing channel is divided intoa plurality of drawing channel members at a position between the openingand the suction pressure generator, each of the drawing channel membersbeing provided with an analytical section and being in communicationwith the suction pressure generator.
 8. A device as claimed in claim 1,wherein the stopper is made from a hydrophobic porous material.
 9. Adevice as claimed in claim 1, wherein the overall length of the deviceis 15 to 100 mm.
 10. A device as claimed in claim 1, wherein the widthof the device is 20 to 50 mm.
 11. A device as claimed in claim 1,wherein the width of the device is 5 to 20 mm.
 12. A device as claimedin claim 1, wherein the overall thickness of the device is 1 to 5 mm.13. A device as claimed in claim 1 wherein the drawing channel isdivided into a plurality of drawing channel members at a positionbetween the opening and the suction pressure generator.
 14. A device asclaimed in claim 1, wherein the main body is dimensioned to bemanipulates hand.
 15. A device as claimed in claim 1, wherein the deviceis designed to be discarded after a single use.
 16. A device as claimedin claim 1, wherein a liquid pooling portion is formed between theopening and the drawing channel, and an air vent passage branches from aportion of the drawing channel between the liquid pooling portion andthe analytical section, the end of the air vent passage opening to theoutside.
 17. A device as claimed in claim 16, wherein the liquid flowresistance in the air vent passage is larger than the liquid flowresistance in the liquid pooling portion.
 18. A device as claimed inclaim 1, wherein a reagent positioning section, a reagent reactionsection and an analytical section are provided independently in certainpositions in the drawing channel.
 19. A device as claimed in claim 18,wherein a plurality of reagent positioning sections are provided incertain positions in the drawing channel.
 20. A device as claimed inclaim 1, wherein the suction pressure generator means is a suctionpressure generating chamber capable of changing its volume.
 21. A deviceas claimed in claim 20, wherein a vent is formed in the suction pressuregenerating chamber.
 22. A device as claimed in claim 1, furthercomprising a bypass channel formed in the main body and branching fromthe drawing channel at a position between the analytical section and theopening and in communication with the suction pressure generator,wherein the relationship between a liquid flow resistance (X) in a firstportion of the drawing channel between said analytical section and saidsuction pressure generator, a liquid flow resistance (Y) in the bypasschannel and a liquid flow resistance (Z) in a second portion of thedrawing channel between the position at which said bypass channelbranches and said analytical section satisfies the inequality(X)>(Y)>(Z).
 23. A device as claimed in claim 22, wherein the drawingchannel is divided into a plurality of drawing channel members at aposition between the opening and the suction pressure generator, each ofthe drawing channel members being provided with an analytical sectionand being in communication with the suction pressure generator, thebypass channel branching from the drawing channel at a position betweenthe division point and the opening.
 24. A device as claimed in claim 1,wherein the suction pressure generator comprises a chamber formed in themain body in communication with the drawing channel.
 25. A device asclaimed in claim 24, further comprising a flexible cover on the mainbody, whereby changes in pressure in the chamber of the suction pressuregenerator are created by movement of the flexible cover.
 26. A device asclaimed in claim 1, wherein a positive pressure can be generated toreturn a sample withdrawn from the analytical section to the analyticalsection.
 27. A device as claimed in claim 1, further comprising a bypasschannel formed in the-main body and branching from the drawing channelat a position between the analytical section and the opening and incommunication with the suction pressure generator.
 28. A device asclaimed in claim 27, wherein a liquid flow resistance in a first portionof the drawing channel between said analytical section and said suctionpressure generator is greater than a liquid flow resistance in thebypass channel and a liquid flow resistance a second portion of thedrawing channel between said analytical section and a position at whichsaid bypass channel branches.